Perivascular epithelioid cell tumor (PEComa) of the uterus with aggressive behavior at presentation

Perivascular epithelioid cell tumor (PEComa) is a rare mesenchymal tumor composed of histologically and immunohistochemically distinctive perivascular epithelioid cells (PECs). Both benign and malignant tumors have been identified, but the criteria for diagnosis of malignancy have not been fully est...

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Main Authors: Jing-Lan Liu, Yueh-Min Lin, Ming-Chieh Lin, Kun-Tu Yeh, Jui- Chang Hsu, Chih-Jung Chen
Format: Article
Language:English
Published: Elsevier 2009-07-01
Series:Hematology/Oncology and Stem Cell Therapy
Online Access:http://www.sciencedirect.com/science/article/pii/S1658387609500131
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spelling doaj-512e6d642c3247239455aefb3570b44e2020-11-24T22:44:31ZengElsevierHematology/Oncology and Stem Cell Therapy1658-38762009-07-0123426430Perivascular epithelioid cell tumor (PEComa) of the uterus with aggressive behavior at presentationJing-Lan Liu0Yueh-Min Lin1Ming-Chieh Lin2Kun-Tu Yeh3Jui- Chang Hsu4Chih-Jung Chen5Changhua Christian Hospital, Changhua, Taiwan, Province of ChinaChanghua Christian Hospital, Changhua, Taiwan, Province of ChinaChanghua Christian Hospital, Changhua, Taiwan, Province of ChinaChanghua Christian Hospital, Changhua, Taiwan, Province of ChinaChanghua Christian Hospital, Changhua, Taiwan, Province of ChinaCorrespondence: Chih-Jung Chen · Changhua Christian Hospital, Changhua, Taiwan, Province of China; Changhua Christian Hospital, Changhua, Taiwan, Province of ChinaPerivascular epithelioid cell tumor (PEComa) is a rare mesenchymal tumor composed of histologically and immunohistochemically distinctive perivascular epithelioid cells (PECs). Both benign and malignant tumors have been identified, but the criteria for diagnosis of malignancy have not been fully established due to the rarity of the tumor. We report on a case of uterine PEComa in a 33-year old woman with lymph node metastasis at presentation. The tumor had the characteristic histologic features of PEComa with cytologic atypia, mitotic activity of 2/10 high power field (HPF), and necrosis; it exhibited im-munopositivity for HMB-45, calponin and desmin and was negative for melan-A. The patient received neoadjuvant chemotherapy, debulking surgery and adjuvant chemotherapy. No evidence of recurrence or metastasis was apparent 8 months after surgery.http://www.sciencedirect.com/science/article/pii/S1658387609500131
collection DOAJ
language English
format Article
sources DOAJ
author Jing-Lan Liu
Yueh-Min Lin
Ming-Chieh Lin
Kun-Tu Yeh
Jui- Chang Hsu
Chih-Jung Chen
spellingShingle Jing-Lan Liu
Yueh-Min Lin
Ming-Chieh Lin
Kun-Tu Yeh
Jui- Chang Hsu
Chih-Jung Chen
Perivascular epithelioid cell tumor (PEComa) of the uterus with aggressive behavior at presentation
Hematology/Oncology and Stem Cell Therapy
author_facet Jing-Lan Liu
Yueh-Min Lin
Ming-Chieh Lin
Kun-Tu Yeh
Jui- Chang Hsu
Chih-Jung Chen
author_sort Jing-Lan Liu
title Perivascular epithelioid cell tumor (PEComa) of the uterus with aggressive behavior at presentation
title_short Perivascular epithelioid cell tumor (PEComa) of the uterus with aggressive behavior at presentation
title_full Perivascular epithelioid cell tumor (PEComa) of the uterus with aggressive behavior at presentation
title_fullStr Perivascular epithelioid cell tumor (PEComa) of the uterus with aggressive behavior at presentation
title_full_unstemmed Perivascular epithelioid cell tumor (PEComa) of the uterus with aggressive behavior at presentation
title_sort perivascular epithelioid cell tumor (pecoma) of the uterus with aggressive behavior at presentation
publisher Elsevier
series Hematology/Oncology and Stem Cell Therapy
issn 1658-3876
publishDate 2009-07-01
description Perivascular epithelioid cell tumor (PEComa) is a rare mesenchymal tumor composed of histologically and immunohistochemically distinctive perivascular epithelioid cells (PECs). Both benign and malignant tumors have been identified, but the criteria for diagnosis of malignancy have not been fully established due to the rarity of the tumor. We report on a case of uterine PEComa in a 33-year old woman with lymph node metastasis at presentation. The tumor had the characteristic histologic features of PEComa with cytologic atypia, mitotic activity of 2/10 high power field (HPF), and necrosis; it exhibited im-munopositivity for HMB-45, calponin and desmin and was negative for melan-A. The patient received neoadjuvant chemotherapy, debulking surgery and adjuvant chemotherapy. No evidence of recurrence or metastasis was apparent 8 months after surgery.
url http://www.sciencedirect.com/science/article/pii/S1658387609500131
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